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Article

Riboflavin-responsive epilepsy in a patient with SER209 variant form of short-chain acyl-CoA dehydrogenase.

Journal of inherited metabolic disease - 1 Jan 1995

Kmoch S, Zeman J, Hrebícek M, Ryba L, Kristensen M J, Gregersen N

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Share to Acyl-CoA Dehydrogenase
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 7564254
DOI: 10.1007/BF00711774

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026.

Related research

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Click a neighbor to travelStep 1 · 9 closest

Riboflavin-responsive epilepsy in a patient with SER209 variant form of short-chain acyl-CoA dehydrogenase.PMID 7564254Read ↗

A case of late-onset riboflavin responsive multiple acyl-CoA dehydrogenase deficiency with novel mutations in ETFDH gene.Semantic proximity Read ↗

Short-chain and medium-chain acylCoA dehydrogenases are lowered in riboflavin-responsive lipid myopathies with multiple acylCoA dehydrogenase deficiency.Semantic proximity Read ↗

Multiple acyl-coenzyme A dehydrogenation disorders (MAD) responsive to riboflavin: biochemical studies in fibroblasts.Semantic proximity Read ↗

Flavin adenine dinucleotide status and the effects of high-dose riboflavin treatment in short-chain acyl-CoA dehydrogenase deficiency.Semantic proximity Read ↗

Diagnosis of a patient with a kinetic variant of medium and short-chain 3-hydroxyacyl-CoA dehydrogenase deficiency by newborn screening.Semantic proximity Read ↗

Amelioration of acylcarnitine profile using bezafibrate and riboflavin in a case of adult-onset glutaric acidemia type 2 with novel mutations of the electron transfer flavoprotein dehydrogenase (ETFDH) gene.Semantic proximity Read ↗

Riboflavin in Neurological Diseases: A Narrative Review.Semantic proximity Read ↗

Riboflavin treatment in L-2-hydroxyglutaric aciduria: report on a pediatric patient and literature review.Semantic proximity Read ↗

Medium chain acyl-coenzyme A dehydrogenase deficiency in a neonate.Semantic proximity Read ↗

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